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Archives Francaises De Pediatrie|June 1, 1975
[Reverse type of cri du chat disease: 5 p trisomy]C Stoll, M O Rethore, C Laurent, et al.Epilepsia|November 1, 1990
Landau-Kleffner syndrome: a pharmacologic study of five casesC Marescaux, E Hirsch, S Finck, et al.Fetal Diagnosis and Therapy|January 1, 1996
Sirenomelia and situs inversus: case report and review of the literatureB Langer, C Stoll, R Nicolau, et al.Genetic Counseling (Geneva, Switzerland)|October 28, 2003
Multiple congenital malformations including generalized hypertrichosis with gum hypertrophy in a child exposed to valproic acid in uteroC Stoll, F Audeoud, C Gaugler, et al.Environmental Science & Technology|August 1, 2012
Prevalence of clinically relevant antibiotic resistance genes in surface water samples collected from Germany and AustraliaC Stoll, J P S Sidhu, A Tiehm, et al.Journal of Medical Genetics|February 1, 1979
Abnormal children of a 47,XYY fatherC Stoll, E Flori, A Clavert, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Tau syndrome (thrombocytopenia and absent ulnar) with mental retardation and facial dysmorphyC Stoll, S Finck, B Janser, et al.Prenatal Diagnosis|April 1, 1994
Hepatic calcifications in a fetus with trisomy 9 that underwent cordocentesisD Satge, B Gasser, A Geneix, et al.Humangenetik|January 1, 1975
Ring chromosome 15:r(15). Identification by R bandingC Stoll, J G Juif, J C Luckel, et al.Prenatal Diagnosis|January 1, 1991
Prenatal diagnosis of congenital myasthenia with arthrogryposis in a myasthenic motherC Stoll, M C Ehret-Mentre, A Treisser, et al.Pageof 33